Watch the Bateman Horne Center Meeting Livestream

The Bateman Horne Center (BHC) hosts free Education Meetings on the 1st Wed of each month at 7pm mountain time/8pm central via livestream at: http://www.youtube.com/c/OfferutahOrg/live


Wednesday, November 2  |  7pm Mountain  |  Lucinda Bateman, MD
Global Report of Progress                                        

Dr. Lucinda Bateman, BHC Founder and Medical Director, is actively engaged in ME/CFS and FM thought leadership across the globe. In October. she has been on the road to advance the discussions that lead to progress:

  • October 8th – SMCI Scientific Advisory Council meeting,
  • October 17-20 – ME/CFS conference in Sweden, and
  • October 27-30 – 12th International IACFS/ME Research and Clinical Conference: Emerging Science and Clinical Care.

This October, she will connect with hundreds of scientists, physicians, professionals, and patients interested in ME/CFS and Fibromyalgia from around the world. At the November BHC Education Meeting, Dr. B will recap for all the information, insights, progress and promise she has gleaned from these conferences.

Access Dr. Bateman’s full bio HERE


You can access the livestream on November 2 by clicking below:

[button_color url=”http://www.youtube.com/c/OfferutahOrg/live” content=”Click here to livestream” target=”http://www.youtube.com/c/OfferutahOrg/live”]

Facebook
Twitter
WhatsApp
Email

Latest News

blackish rectangle with the words, MEAction Georgia Volunteer - Maggie Boxey- at TEDxOjia with the meaction logo in the bottom right corner.

#MEAction Georgia Volunteer, Maggie Boxey, Speaks at TEDxOjai

#MEAction Georgia recently had a huge accomplishment. Maggie Boxey, who is a member of the Georgia State Chapter, a Navy veteran, and a published author, recently gave a Tedx talk about her experience as a person with ME. Maggie was diagnosed a year ago but has been sick since 2020. Before becoming sick Maggie and

Read More »

SOS: Save our Science

People disabled by ME and Long Covid across the UK send out an SOS.  It’s time to send out our SOS signal, if we want to have funded research. May 12th, is Myalgic Encephalomyelitis Awareness Day. On this day, the #MillionsMissing of people with myalgic encephalomyelitis (ME) gather to demand an increase in research and

Read More »
a blue square image that features waves as the background. The 2025 #MillionsMissing logo at the top. followed by the words, Why We're sending out an SOS. A life preserver is in the bottom right corner and the meaction logo is in the bottom left corner.

Why We’re Sending out an SOS this #MillionsMissing

On May 12th, #MEAction and the #MillionsMissing are sending out an SOS to Congress to Save our Support Systems. Save our Science. Save Our Society.  HERE’S WHY: Healthcare, research funding and accessibility were already incredibly fragile for people with myalgic encephalomyelitis (ME), Long Covid and the disability communities. Now, we are seeing constant threats to

Read More »